... and contribute to submission strategy, regulatory dossiers, and safety issues. You proactively identify the need of studies, which need to be conducted, and you provide input to Medical Affairs strategy documents such as Scientific ...
... our team as Application Support Manager m f d for our ... . As a European Teamcenter Support Manager, you will lead Application Support ... Sales and Services, Customer Success Managers, and Product Development in the ...
... , office-based Associate Clinical Trial Manager (aCTM) to join our Clinical ... Project Coordinators and Clinical Trial Managers in performance of clinical trial ... quality control of our internal regulatory filing system Provide oversight and ...
... in Munich, Germany. Clinical Trial Managers with expertise in CNS and ... preferred; 5+ years of Project Manager Clinical Trial Manager experience at a CRO required ... disciplined approach. We leverage local regulatory and therapeutic expertise across all ...
... , office-based Associate Clinical Trial Manager (aCTM) to join our Clinical ... Project Coordinators and Clinical Trial Managers in performance of clinical trial ... quality control of our internal regulatory filing system Provide oversight and ...
... Zeitpunkt einen Sachbearbeiter HR & General Affairs (w m d).Bei der ... Aufgaben als Sachbearbeiter HR & General Affairs (w m d)Betreuung eines ...
... respective internal colleagues within Medical Affairs, Clinical Development, Market Access, and ... in malignant hematology. You have drug launch experience and are knowledgeable ... supervision while adhering to compliance regulatory policies. You are capable of ...
... respective internal colleagues within Medical Affairs, Clinical Development, Market Access, and ... in malignant hematology. You have drug launch experience and are knowledgeable ... supervision while adhering to compliance regulatory policies. You are capable of ...
... respective internal colleagues within Medical Affairs, Clinical Development, Market Access, and ... in malignant hematology. You have drug launch experience and are knowledgeable ... supervision while adhering to compliance regulatory policies. You are capable of ...
... GCP ICH guidelines and other regulatory requirements. This includes effective communication ... timely completion of both drug and non-drug program goals and objectives Generate ... direction of a Global SSU Manager including CDA and questionnaire collection, ...